| 초록 |
Structure-property relationship was studied for fully aliphatic polyimides containing alicyclic dianhydride and diamine units. Rel-(1'R,3S,5'S)-spiro[furan-3(2H),6'-[3]oxabicyclo[3.2.1]octane]-2,2',4',5(4H)-tetrone (DAn) was used as an unsymmetrical spiro dianhydride, and 1,2,3,4-cyclopentanetetracarboxylic dianhydride (CPDA) and bicyclo[2.2.2]oct-7-ene-2,3,5,6-tetracarboxylic dianhydride (BOCA) were used as symmetrical non-spiro dianhydrides. 4,4’-Methylenebis(2-methylcyclohexylamine) (MMCA) and 5-amino-1,3,3-trimethylcyclohexanemethylamine (AMCH) were N-silylated and reacted with the dianhydrides to prepare the fully alicyclic polyimides. The formation of the polyimides were confirmed by FT-IR spectroscopy. The DAn-based polyimides showed higher solubility than the polyimides derived from CPDA or BOCA. This was explained based on the results of wide-angle X-ray diffraction (WAXD) analysis of the polyimides. |
